Catalog Number

-

Brand Name

NONE

Version/Model Number

NONE

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 15, 2019

Issuing Agency

In HIBCC

MRI safety Status

MR Unsafe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K121931

Product Code

ETN

Product Code Name

Stimulator, Nerve

Public Device Record Key

fc061eab-49dc-4b56-bd64-ceb9dea02946

Public Version Date

October 15, 2021

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-